Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,551–7,600 of 15,271
- Class II
Drug Recall · March 11, 2025
Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, package in 5 mL bottles, Rx Only, Distributed by: Leading Pharma LLC, Fairfield, NJ. Manufactured by: FDC Limited, Maharashtra, India, NDC 69315-30Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
- Unclassified
Vehicle Recall · March 11, 2025
2025 MACK GRANITE (GR)Loss of headlight illumination can reduce visibility, increasing the risk of a crash.
- Unclassified
Vehicle Recall · March 11, 2025
2026 VOLVO VNL (4)Marker lights that fail to illuminate can reduce visibility to other drivers, increasing the risk of a crash.
- Class I
Medical Device Recall · March 11, 2025
BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196, 9174118, CK000955, 3174135, CK000617, CK000839, 3194355, 6174118, 3194135, 3194335, 217Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.
- Class I
Food Recall · March 11, 2025
Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook through beforeContaminated with Listeria monocytogenes
- Class III
- Class II
Drug Recall · March 11, 2025
CVS Health Concealing Acne Treatment Cream, CVS, 10% benzoyl peroxide, 1 oz (28 g), Distributed by: CVS Pharmacy, IncChemical contamination: presence of benzene
- Class II
Medical Device Recall · March 11, 2025
Siemens Healthcare Diagnostics, Inc.
Atellica CH Revised C Reactive Protein (RCRP); Siemens Material Number (SMN): 11537223.Incorrect software flagging may occur for the assay that may potentially lead to an erroneous result.
- Class II
Drug Recall · March 11, 2025
Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl Peroxide/Acne Medication, 0.65 oz (18.4g) tube in a carton; Distributed by: Walgreen CO., 200 Wilmot Rd., Deerfield, IL 60015Chemical contamination: presence of benzene
- Class II
Medical Device Recall · March 11, 2025
BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated dispensing cabinets (ADC) intended to securely store and dispense medications to a quaDue to a software bug, automated dispensing cabinet is unable to calculate countback discrepancies during the issue process, which causes incorrect transaction quantity to be recorded. This bug can also result in the CUBIE opening more times than needed for the transaction to be completed, which may result in a patient receiving more than the intended dose of medication.
- Class II
Medical Device Recall · March 11, 2025
BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI 1HH-1HM-1FM, 169-102; MINI 2FH, 138902-01; MINI 2FH, 169-104; MINI 2FM, 169-105;Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock transactions and 2 stock transactions, which results in doubling the bin quantity, which may result in a delay in access to desired medications and/or supplies, which may lead to temporary body function impairment.
- Class II
Drug Recall · March 11, 2025
Glenmark Pharmaceuticals Inc., USA
chlorproMAZINE Hydrochloride Tablets, USP 100 mg, Rx Only, 100 Tablets per bottle, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Product of India, NDC 68462-864-01CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit.
- Unclassified
Vehicle Recall · March 11, 2025
2023 VOLVO VAHA seat belt anchor that fails will not properly restrain an occupant in a crash, increasing the risk of injury.
- Class I
Food Recall · March 11, 2025
365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482499709. Distributed by: Whole Foods Market, Austin, TXUndeclared allergen (eggs) and pork
- Class II
Medical Device Recall · March 11, 2025
BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P / 155141-01 BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P / 155140-01 BD PYXIS MEDBANK TWR MN CR-Due to a software issue, when attempting to restock the automated dispensing cabinet, user have received the banner message "Stocking window has passed, or item has been removed from purchase order. Please contact Pharmacy for assistance". When this occurs, the medication cannot be restocked and can potentially lead to delays in accessing medication for patients.
- Unclassified
Vehicle Recall · March 10, 2025
2024 HOLIDAY RAMBLER INVICTAA propane gas leak increases the risk of a fire.
- Class I
Food Recall · March 10, 2025
Zaarah Herbals brand Vasaka Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99967 0Products contain elevated levels of Lead (Pb): 6.504 ppm
- Class II
Medical Device Recall · March 10, 2025
Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.
- Class II
Medical Device Recall · March 10, 2025
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED, REF: NIM4CM01RF; PATIENT INTERFACE NIM4CPB1 NIM 4.0, REF: NIM4CPB1; PATIENNerve Monitoring System with certain software versions has potential for increased stimulus artifact, which may require troubleshooting, and may lead to procedure delay, extubation, and medical intervention.
- Class II
Medical Device Recall · March 10, 2025
Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.Potential for collimator to fall as a result of incorrect installation.
- Class I
Food Recall · March 10, 2025
Zaarah Herbals brand Rasayan Churan; packaged in 100g clear jars with gold lids; UPC:6 35028 99966 3Products contain elevated levels of Lead (Pb): 88.038 ppm
- Class I
Food Recall · March 10, 2025
Zaarah Herbals brand Bhringraj Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99973 1Products contain elevated levels of Lead (Pb): 3.231 ppm and Arsenic (As): 0.958 ppm;
- Class I
Food Recall · March 10, 2025
Zaarah Herbals brand Gurmar Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99969 4Products contain elevated levels of Lead (Pb): 3.688 ppm
- Class II
Food Recall · March 10, 2025
Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per day with meals, Distributed by: McDonagh Medical Center Gladstone, MO 64119Levels of iodine exceeding label claim
- Class II
Medical Device Recall · March 10, 2025
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.Potential for collimator to fall as a result of incorrect installation.
- Unclassified
Vehicle Recall · March 9, 2025
2023 DUCATI PANIGALE V4A rear wheel axle that breaks while riding can result in a loss of motorcycle control, increasing the risk of a crash or injury.
- Class II
Medical Device Recall · March 8, 2025
TLX/TLC SP Guided Implant Driver, for ratchet, stainless steel; REF: 037.3002;The devices are missing the laser marked depth markings.
- Class II
Medical Device Recall · March 7, 2025
PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MPIdentified curing issues with the silicone during the needles manufacturing process.
- Class II
Drug Recall · March 7, 2025
Duloxetine D/R, 20 mg, 30 Caps, 30-count bottle, RX Only, Packaged & Distributed by: Direct Rx, Dist. By Breckenridge Pharm., Inc., Berlin, CT 06037, NDC 61919-422-30CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
- Class II
Drug Recall · March 7, 2025
Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in InSuper-Potent Drug: Out of specification potency results were obtained.
- Class II
Drug Recall · March 7, 2025
Cinacalcet Hydrochloride Tablets 60 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-008-04CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
- Class II
Drug Recall · March 7, 2025
Consumer Product Partners, LLC
[CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution, USP, 32 FL OZ (1 QT) 946 mL per bottle, NDC 0869-0871-45; [INCORRECT BACK LABEL] Isopropyl alcohol 91%, Dist. by: Amazon.com Services, LLC, SeLabeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
- Class II
Drug Recall · March 7, 2025
8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL (1 mEq/mL), 25 x 50 mL Single Dose Vials per carton, For Intravenous Use Only, Rx Only, Manufactured by: Exela Pharma Sciences, LLC, Lenoir, NC 286Lack of Assurance of Sterility
- Class II
Medical Device Recall · March 7, 2025
ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MHIdentified curing issues with the silicone during the needles manufacturing process.
- Class II
Drug Recall · March 7, 2025
Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
- Class II
Drug Recall · March 7, 2025
Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per carton, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, Made in IndSuper-Potent Drug: Out of specification potency results were obtained.
- Class II
Drug Recall · March 7, 2025
Duloxetine D/R, 30 mg, 30 Caps, RX Only, Packaged as a) 30-count bottle NDC 61919-0482-30, b) 60-count bottle, NDC 61919-0482-60, c) 90-count bottle, NDC 61919-0482-90; Packaged & Distributed by: DiCGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
- Class II
Medical Device Recall · March 7, 2025
PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1Identified curing issues with the silicone during the needles manufacturing process.
- Class II
Drug Recall · March 7, 2025
Sofosbuvir and Velpatasvir, 400 mg/100 mg tablets, 28 tablets: 2x14 blister cards, Rx Only, Manufactured for: Asegua Therapeutics LLC an affiliate of Gilead Sciences, Inc., Foster City, CA 94404, MadeDefective Container: blister packs not properly sealed resulting in tablets being loose in the carton.
- Class II
Medical Device Recall · March 7, 2025
PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRMIdentified curing issues with the silicone during the needles manufacturing process.
- Unclassified
Vehicle Recall · March 6, 2025
2023 RIVIAN R1T, 2023 RIVIAN R1S, 2024 RIVIAN R1T, 2024 RIVIAN R1S, 2025 RIVIAN R1T, 2025 RIVIAN R1SAn improperly secured seat belt may not restrain an occupant as intended, increasing the risk of injury during a crash.
- Class II
Medical Device Recall · March 6, 2025
Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays.The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
- Unclassified
Consumer Product Recall · March 6, 2025
Marie-Chantal Ltd., of United Kingdom
Marie-Chantal Children's Nightgowns, Pajama Sets and RobesThe recalled children's nightgowns, pajama sets and robes violate the federal flammability standards for children's sleepwear, posing a risk of serious burn injuries or death to children.
- Unclassified
Consumer Product Recall · March 6, 2025
Taylor Water Technologies LLC, of Sparks, Maryland
Phosphate Reagent #1 Bottles sold within the Taylor Phosphate Test KitsThe recalled Taylor Water Technologies reagent bottles sold with test kits contain sulfuric acid, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The packaging for the bottle with sulfuric acid is not child resistant, posing a risk of chemical burns to the skin or eyes and internal corrosive burns, if ingested.
- Class II
Drug Recall · March 6, 2025
fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine HCl 100 mg/100 mL (1 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For InstitLack of Assurance of Sterility
- Class II
Medical Device Recall · March 6, 2025
Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG), R5 (Model Numbers H45135VG, H45135VGW), R3 Surgery for China (Model Number H45113VGSU), R3 PeriOP fThe battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
- Unclassified
Vehicle Recall · March 6, 2025
2023 FORD ESCAPE, 2024 FORD ESCAPEAn oil leak can result in loss of drive power, increasing the risk of a crash. In addition, an oil leak in the presence of an ignition source such as hot engine or exhaust components, can increase the risk of a fire.
- Class II
Food Recall · March 6, 2025
Great Lakes Coca-Cola Distribution LLC
Coco-Cola Original Taste, 12 Fl Oz. (355mL). Can UPC 0 49000-00634 6. 12-can pack UPC 0 49000-02890 4. Canned Under Authority of the Coca-Cola Company, Atlanta, GA 30313.Foreign object (plastic)
- Class II
Drug Recall · March 6, 2025
fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine HCl 200 mg/100 mL (2 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For InstitLack of Assurance of Sterility
- Class II
Medical Device Recall · March 6, 2025
Venue Fit Models: R3 (Model Number H45303VFSC, H45303VFSW), R4 (Model Number H45314VFS, H45314VFSW), Venue Fit R5 system (Model Numbers H45335VFS, H45335VFSW), R3 Surgery for China, R3 PeriOP for ChinThe battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.